Skip to content

Pediatric Relapsing Polychondritis : Diagnosis and Management in a French Retrospective Study

Pediatric Relapsing Polychondritis : Diagnosis and Management in a French Retrospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06019221
Acronym
PRP
Enrollment
20
Registered
2023-08-31
Start date
2023-02-18
Completion date
2024-01-18
Last updated
2023-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsing Polychondritis

Keywords

Polychondritis, Relapsing Polychondritis, Pediatric Relapsing Polychondritis

Brief summary

The incidence in pediatrics is very low (about 3.5 per million per year according to a 2015 study) and therefore the data on the pathology very poor, especially on the therapeutic level. Without appropriate treatment, the disabling sequelae, even involving the vital prognosis, are significant. However, in paediatrics, therapeutic habits have been extrapolated from adult data and lack precision. Existing treatments are almost composed of immunomodulatory and/or immunosuppressive treatments. Different therapeutic lines have been introduced over the years and a better understanding of the pathology. More recently, biotherapies have been introduced in this pathology, but data on their effectiveness remain limited. Data on the evolution under therapy in children are thus still poor. Complications related to the pathology that can jeopardize the vital prognosis and the response to treatment for this pathology deserve to be studied in order to be known and if possible avoided. The aim of the study is to describe French practices and compare the lines of treatment proposed for juvenile atrophic polychondritis.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Minor subject aged 1 to 17 years * Diagnosis of atrophic polychondritis between 01/01/2008 to 31/12/2022. * Subject (and/or his parental authority) who has not expressed, after being informed, his opposition to the reuse of his data for the purposes of this research.

Exclusion criteria

* Subject (or his parents) having expressed his (their) opposition to participating in the study * Associated pathologies that cannot be related to the diagnosis of atrophic polychondritis and whose prognosis can lead to biases in the efficacy and/or complications related to treatments.

Design outcomes

Primary

MeasureTime frameDescription
Therapeutic effectiveness of the various treatments proposed depending on the degree of initial clinical involvementFiles analysed retrospectively from from January 01, 2008 to December 31, 2022 will be examinedThe aim of this study is to bring together the experiences of the various reference and competence centers in France concerning the clinical presentation, management and follow-up of children with relapsing polychondritis.

Countries

France

Contacts

Primary ContactAriane ZALOSZYC, MD
ariane.zaloszyc@chru-strasbourg.fr33 3 88 12 77 42
Backup ContactSarah-Louisa MAHI, MD
sarah-louisa.mahi@chru-strasbourg.fr33 3 88 12 77 42

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026